Affiliation:
1. State Key Laboratory of Power Grid Environmental Protection; Hubei Key Lab on Organic and Polymeric Optoelectronic Materials; Engineering Research Center of Organosilicon Compounds & Materials, Ministry of Education; Key Laboratory of Biomedical Polymers of Ministry of Education & College of Chemistry and Molecular Sciences, Wuhan University Wuhan Hubei 430072 China
Abstract
Comprehensive SummaryThe first asymmetric hydrogenation of acyclic tetrasubstituted α,β‐unsaturated amides has been achieved by using Rh/DuanPhos complex as a catalyst, delivering chiral β‐amino amides with two contiguous chiral centers in excellent yields and high enantioselectivities (up to 99% yield, 96% ee), which provides efficient and concise access to valuable β‐amino amide derivatives. The gram‐scale reaction and efficient transformation of β‐amino amide to β‐amino acid and β‐amino cyanide demonstrated the utility of this methodology.
Funder
National Natural Science Foundation of China
Cited by
1 articles.
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